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170640-75-2

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170640-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 170640-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,6,4 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 170640-75:
(8*1)+(7*7)+(6*0)+(5*6)+(4*4)+(3*0)+(2*7)+(1*5)=122
122 % 10 = 2
So 170640-75-2 is a valid CAS Registry Number.

170640-75-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name S-[(4-nitrophenyl)methyl] ethanethioate

1.2 Other means of identification

Product number -
Other names S-(4-nitrophenylmethyl)thioacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:170640-75-2 SDS

170640-75-2Relevant articles and documents

Near-IR mediated intracellular uncaging of NO from cell targeted hollow gold nanoparticles

Levy, Elizabeth S.,Morales, Demosthenes P.,Garcia, John V.,Reich, Norbert O.,Ford, Peter C.

, p. 17692 - 17695 (2015)

We demonstrate modulation of nitric oxide release in solution and in human prostate cancer cells from a thiol functionalized cupferron (TCF) absorbed on hollow gold nanoshells (HGNs) using near-infrared (NIR) light. NO release from the TCF-HGN conjugates

Convenient synthesis of alkyl thioacetate from alkyl halide using a polymer-supported sodium thioacetate

Zarchi, Mohammad Ali Karimi,Nejabat, Mojgan

, p. 767 - 774 (2013/02/23)

Alkyl halides are efficiently converted to their corresponding S-alkyl thioacetates under mild and nonaqueous conditions, using polymer-supported sodium thioacetate as a new polymeric reagent at room temperature in high yields and purity. The spent polymeric reagent can be removed quantitatively by filtration and pure products can be obtained by evaporation of the solvent. The spent polymeric reagent can be regenerated and reused several times without its activity changing appreciably. Iranian Chemical Society 2012.

Probing the mechanism of electron capture and electron transfer dissociation using tags with variable electron affinity

Sohn, Chang Ho,Chung, Cheol K.,Yin, Sheng,Ramachandran, Prasanna,Loo, Joseph A.,Beauchamp, J. L.

experimental part, p. 5444 - 5459 (2009/09/25)

Electron capture dissociation (ECD) and electron transfer dissociation (ETD) of doubly protonated electron affinity (EA)-tuned peptides were studied to further illuminate the mechanism of these processes. The model peptide FQpSEEQQQTEDELQDK, containing a

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